Cleared Traditional

K952101 - MARQUETTE DEFIB ELECTRODES

K952101 is the FDA 510(k) clearance for MARQUETTE DEFIB ELECTRODES by Marquette Electronics, Inc.. It is a Class 3 Cardiovascular device (product code MKJ) cleared through the Traditional 510(k) pathway after a 126-day FDA review.

K952101 · Marquette Electronics, Inc. · Cardiovascular device
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Sep 1995
Decision
126d
Days
Class 3
Risk

K952101 is an FDA 510(k) clearance for the MARQUETTE DEFIB ELECTRODES. Classified as Automated External Defibrillators (non-wearable) (product code MKJ), Class III - Premarket Approval.

Submitted by Marquette Electronics, Inc. (Jupiter, US). The FDA issued a Cleared decision on September 7, 1995 after a review of 126 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.5310 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: High-complexity regulatory submission. High regulatory complexity profile. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Marquette Electronics, Inc. devices

Submission Details

510(k) Number K952101 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 04, 1995
Decision Date September 07, 1995
Days to Decision 126 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
1d slower than avg
Panel avg: 125d · This submission: 126d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code MKJ Automated External Defibrillators (non-wearable)
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 870.5310
Definition This Device Is A Non-wearable Prescription Use Only Aed. These Are Devices That Include Automated External Defibrillation. Automated External Defibrillators Use External Pad-type Electrodes To Sense, Detect, Classify And Treat (with An Electrical Shock) Ventricular Fibrillation. These Devices Are Intended To Be Used On Suspected Victims Of Sudden Cardiac Arrest. A Person In Cardiac Arrest Is Unresponsive And Is Not Breathing Normally. The Device Can Be Sold With Prescription Only.
What this classification means

Class III devices typically require Premarket Approval (PMA) with clinical evidence. Clearance through 510(k) for Class III devices is granted only when substantial equivalence to a valid predicate can be established.

Regulatory Peers - MKJ Automated External Defibrillators (non-wearable)

All 87
Devices cleared under the same product code (MKJ) and FDA review panel - the closest regulatory comparables to K952101.
MEDI-TRACE COMBINATION DEFIBRILLATION & ECG ELECTRODE FOR PHYSIO CONTROL DEFIBRILLATORS
K955828 · Graphic Controls Corp. · Jul 1996
CODEMASTER XL + XL W/SHOCK ADVISORY OPTION
K954957 · Hewlett-Packard Co. · May 1996
PEDIATRIC QUIK-COMBO
K953204 · Physio-Control Corp. · Jan 1996
MARQUETTE DEFIB ELECTRODE
K941262 · Marquette Electronics, Inc. · Apr 1995
ZOLL PD 1600 SEMI-AUTOMATIC EXTERNAL DEFIBRILLATOR
K942344 · Zoll Medical Corp · Mar 1995
ZOLL POWERBASE(TM)
K942850 · Zoll Medical Corp · Feb 1995